Additional glycoprotein abnormalities in a rare type of thrombasthenia

Molecular analysis of FVIII gene in severe HA patients of Costa Rica.

Hamostaseologie·2010

Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene.

Haemophilia : the official journal of the World Federation of Hemophilia·2008

Molecular diagnosis of hemophilia A and B. Report of five families from Costa Rica.

Revista de biologia tropical·2007

Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene.

Haemophilia : the official journal of the World Federation of Hemophilia·2006

Long-term FVII substitution in a preterm infant with severe gastrointestinal bleeding and FVII deficiency due to a homozygous donor splice mutation IVS4+1G-->A.

Pediatric hematology and oncology·2006

Biochemical indicators of nutritional status and dietary intake in Costa Rican Cabécar Indian adolescents.

Food and nutrition bulletin·2005

Substitution-induced allosteric activation of coagulation factor IX as a potential alternative hemophilia A treatment strategy.

Thrombosis research·2026

Development and external validation of a text-matching algorithm to identify patients with lower extremity deep venous thrombosis from radiology reports at five medical centers.

Thrombosis research·2026

Predicting chronic immune thrombocytopenia in children using IFNA17 rs9298814 polymorphism and clinical features: a study from a low- and middle-income country.

Thrombosis research·2026

Long-term analytical performance of apixaban measurements based on external quality assessment data.

Thrombosis research·2026

Safety and efficacy of fondaparinux in pediatric venous thromboembolism: A retrospective cohort study.

Thrombosis research·2026

Phenotypic and glycosylation profiles of the FGG c.902G > A (p.Arg301His) mutation in a Chinese pedigree with congenital dysfibrinogenemia.

Thrombosis research·2026

Managing Acute STEMI in the Setting of Immune Thrombocytopenic Purpura: A Therapeutic Dilemma.

JACC. Case reports·2026

Staged matrix and micrografting reconstruction for no-option CLTI: A case report.

Science progress·2026

Management of Acute Coronary Syndromes: Is the Yentl Syndrome Vanishing?

Journal of the American Heart Association·2026

Golidocitinib as salvage therapy before allogeneic hematopoietic stem cell transplantation in refractory Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis.

Haematologica·2026

Unmasking coronary embolism: rare non-atherosclerotic causes of acute coronary syndrome in the young: case series.

European heart journal. Case reports·2026

Fatal Delayed Stent-edge Rupture Confirmed by Autopsy after Stent-assisted Coil Embolization for a Blood Blister-like Aneurysm.

NMC case report journal·2026

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Additional glycoprotein abnormalities in a rare type of thrombasthenia

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Molecular analysis of FVIII gene in severe HA patients of Costa Rica.

Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene.

Molecular diagnosis of hemophilia A and B. Report of five families from Costa Rica.

Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene.

Long-term FVII substitution in a preterm infant with severe gastrointestinal bleeding and FVII deficiency due to a homozygous donor splice mutation IVS4+1G-->A.

Biochemical indicators of nutritional status and dietary intake in Costa Rican Cabécar Indian adolescents.

Substitution-induced allosteric activation of coagulation factor IX as a potential alternative hemophilia A treatment strategy.

Development and external validation of a text-matching algorithm to identify patients with lower extremity deep venous thrombosis from radiology reports at five medical centers.

Predicting chronic immune thrombocytopenia in children using IFNA17 rs9298814 polymorphism and clinical features: a study from a low- and middle-income country.

Long-term analytical performance of apixaban measurements based on external quality assessment data.

Safety and efficacy of fondaparinux in pediatric venous thromboembolism: A retrospective cohort study.

Phenotypic and glycosylation profiles of the FGG c.902G > A (p.Arg301His) mutation in a Chinese pedigree with congenital dysfibrinogenemia.

Managing Acute STEMI in the Setting of Immune Thrombocytopenic Purpura: A Therapeutic Dilemma.

Staged matrix and micrografting reconstruction for no-option CLTI: A case report.

Management of Acute Coronary Syndromes: Is the Yentl Syndrome Vanishing?

Golidocitinib as salvage therapy before allogeneic hematopoietic stem cell transplantation in refractory Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis.

Unmasking coronary embolism: rare non-atherosclerotic causes of acute coronary syndrome in the young: case series.

Fatal Delayed Stent-edge Rupture Confirmed by Autopsy after Stent-assisted Coil Embolization for a Blood Blister-like Aneurysm.

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Additional glycoprotein abnormalities in a rare type of thrombasthenia

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